Mepolizumab for COPD Hospital Eosinophilic Admissions Pragmatic Trial

NCT ID: NCT04075331

Last Updated: 2024-07-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 238 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-09-07
• Study Completion Date: 2024-06-21

Brief Summary

This is a single-centre, double-blinded, randomised, placebo controlled trial comparing mepolizumab 100mg versus placebo in patients with eosinophilic COPD, started following their index admission to hospital.

Detailed Description

Patients admitted to hospital with an exacerbation of COPD are at high risk of readmission, of which a proportion are driven by eosinophilic inflammation. Whilst oral corticosteroids are beneficial in exacerbations, a considerable proportion of patients experience treatment failure, with 50% of patients readmitted within 3 months (www.RCPLondon.ac.uk).

Therapy, such as mepolizumab, reduces eosinophil count and has been shown to reduce exacerbation frequency when given in the stable state in both eosinophilic asthma (Papi et al. 2018) and COPD (Yousef, in press).

The investigators hypothesise that starting mepolizumab at the time of a hospitalisation for an exacerbation of COPD in patients with significant eosinophilia will result in a reduction in readmission to hospital in a high risk population.

Therefore, 238 participants will be recruited over an 18-month period and will be randomised into a 48-week treatment period in which they will receive monthly subcutaneous injections of either 100 mg mepolizumab or placebo. Secondary outcomes will be measured at baseline (week 0), 4 weeks, 8 weeks, 12 weeks, 24 weeks, 36 weeks and 48 weeks.

Conditions

COPD; Eosinophilia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Mepolizumab

Mepolizumab

Group Type: EXPERIMENTAL

Mepolizumab

Intervention Type: DRUG

Mepolizumab 100mg subcutaneous injection

Placebo

Saline solution

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Saline solution for subcutaneous injection

Interventions

Mepolizumab

Mepolizumab 100mg subcutaneous injection

Intervention Type: DRUG

Placebo

Saline solution for subcutaneous injection

Intervention Type: DRUG

Other Intervention Names

Saline solution

Eligibility Criteria

Inclusion Criteria

1. Symptoms typical of COPD when stable (baseline eMRC dyspnoea grade 2 or more).

2. A clinician defined exacerbation of COPD requiring admission to hospital.

3. Serum eosinophil count of ≥ 300 cells/μL either at time of admission or at any one time in the preceding 12 months.

4. Smoking pack years ≥10 years.

5. Age ≥ 40 years.

6. Established on inhaled corticosteroids (ICS) prior to this admission.

7. Willing and able to consent to participate in trial.

8. Able to understand written and spoken English.

Exclusion Criteria

1. COPD patients without eosinophilia (defined as persistently < 300 cells/μL within the last 12 months).

2. Other conditions that may be the cause of eosinophilia (such as hypereosinophilic syndrome, eosinophilic granulomatosis, eosinophilic oesophagitis or parasitic infection).

3. Patients whose treatment is considered palliative (life expectancy < 6 months).

4. Other respiratory conditions including active lung cancer, interstitial lung disease, primary pulmonary hypertension or any other conditions that in the view of the investigator will affect the trial.

5. Known history of anaphylaxis or hypersensitivity to mepolizumab or any of the excipients (sucrose, sodium phosphate dibasic heptahydrate, polysorbate 80).

6. Unstable or life-threatening cardiac disease including myocardial infarction or unstable angina in the last 6 months, unstable or life-threatening cardiac arrhythmia requiring intervention in the last 3 months and New York Heart Association (NYHA) Class IV heart failure.

7. Decompensated liver disease or cirrhosis.

8. Pregnant, breastfeeding, or lactating women. Women of child-bearing potential must agree to use appropriate methods of birth control and have a negative blood serum pregnancy test performed after randomisation but prior to first dosing with randomised treatment.*

9. Participation in an interventional clinical trial within 3 months of visit 1 or receipt of any investigational medicinal product within 3 months or 5 half-lives.

10. Known blood born infection (e.g. HIV, hepatitis B or C).

• Women of child bearing potential (WOCBP) - A woman is defined as being of childbearing potential (WOCBP), i.e. fertile, following menarche and until becoming post-menopausal, unless permanently sterile. Permanent sterilisation methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy. A postmenopausal state is defined as no menses for 12 months without an alternative medical cause.

• Minimum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

GlaxoSmithKline

INDUSTRY

Sponsor Role: collaborator

University of Leicester

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Christopher Brightling

Role: STUDY_CHAIR

University of Leicester

Neil Greening

Role: PRINCIPAL_INVESTIGATOR

University of Leicester

Locations

NIHR Biomedical Research Centre, Respiratory

Leicester, Leicestershire, United Kingdom

Countries

United Kingdom

References

Flynn CA, McAuley HJC, Elneima O, Aung HWW, Ibrahim W, Ward TJC, Bourne M, Thornton TD, Mistry V, Gilbert HR, Waheed G, Wright AKA, Evans RA, Steiner MC, Brookes CL, Brightling CE, Greening NJ. Mepolizumab for COPD with Eosinophilic Phenotype following Hospitalization. NEJM Evid. 2025 Jun;4(6):EVIDoa2500012. doi: 10.1056/EVIDoa2500012. Epub 2025 Apr 30.

Reference Type: DERIVED

PMID: 40305842 (View on PubMed)

Other Identifiers

0690

Identifier Type: -

Identifier Source: org_study_id